Ammonia → Methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoate

A solution of methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoate (9.9 g, 27.4 mmol) in DCM (120 mL) was treated with oxalyl chloride (2.59 mL, 30.2 mmol) and the mixture was stirred at RT for 30 min. FeCl3 (5.34 g, 32.9 mmol) was then added portionwise at 0° C. and the resulting brown mixture was stirred at RT for 4 h. A 2N aqueous solution of HCl (35 mL) was then added and the mixture was stirred at RT for another 2 h. The mixture was then diluted with H2O and extracted with DCM. The combined org. phases were then dried over Na2SO4, filtered and concentrated in vacuo. The brown residue obtained was taken up in a 19:1 mixture of MeOH/H2SO4 (120 mL) and stirred at reflux for 3 h. The mixture was then concentrated in vacuo and the brown reside obtained was taken up in H2O. The mixture was rendered basic with ammonia and then extracted with AcOEt. The combined org. phases were dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (SiO2, cHex/AcOEt 100:0 to 70:30) gave the title compound (1.15 g) as yellow oil. UPLC-MS: MS 344.1 (M+H+); UPLC rt 0.96 min.

1. stirringthe resulting brown mixture was stirred at RT for 4 h
2. stirringthe mixture was stirred at RT for another 2 h
3. extractionextracted with DCM
4. dry with materialphases were then dried over Na2SO4
5. filtrationfiltered
6. concentrationconcentrated in vacuo
7. customThe brown residue obtained
8. stirringstirred
9. temperatureat reflux for 3 h
10. concentrationThe mixture was then concentrated in vacuo
11. customthe brown reside obtained
12. extractionextracted with AcOEt
13. dry with materialphases were dried over Na2SO4
14. filtrationfiltered
15. concentrationconcentrated in vacuo
16. customPurification by flash chromatography (SiO2, cHex/AcOEt 100:0 to 70:30)

ORD-Eintrag

ord-0ca03d1b97484d15b3676085b7b7a6ac

Quelldatensatz

uspto-grants-2014_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08853203B2